Canonical Allele Identifier: CA1868275428
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421695G= , CM000671.2:g.101421695G= GRCh38
NC_000009.11:g.104183977G= , CM000671.1:g.104183977G= GRCh37
NC_000009.10:g.103223798G= NCBI36
NG_012387.1:g.19086C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*114C= MANE Select ENSP00000497767.1:n.*114C=
ENST00000648064.1:c.*114C= ENSP00000497990.1:n.*114C=
ENST00000648758.1:c.*114C= ENSP00000497731.1:n.*114C=
ENST00000374855.8:c.*114C= ENSP00000363988.4:n.*114C=
ENST00000616752.1:c.*221C= ENSP00000481363.1:n.*221C=
NM_000035.3:c.*114C= NP_000026.2:n.*114C=
NM_000035.4:c.*114C= MANE Select NP_000026.2:n.*114C=